Preboost 4 g/100mL
benzocaine · LIQUID · The Female Health Company d/b/a Veru Healthcare
Preboost is a topical liquid containing benzocaine that is applied directly to the skin to numb and relieve pain or itching in the treated area. It is available over-the-counter without a prescription.
Key Facts
- Brand Name
- Preboost
- Generic Name
- benzocaine
- NDC Code (Product)
69681-432- Manufacturer
- The Female Health Company d/b/a Veru Healthcare
- Strength
- 4 g/100mL
- Dosage Form
- LIQUID
- Route
- TOPICAL
- Marketing Status
- Application #
- part348
- Drug Class
- Standardized Chemical Allergen [EPC]
- Marketing Start
- 03/30/2015
Recall History
No Recall HistoryFrequently Asked Questions
What is Preboost used for?
Preboost is a topical liquid containing benzocaine that is applied directly to the skin to numb and relieve pain or itching in the treated area. It is available over-the-counter without a prescription.
Is Preboost a controlled substance?
Preboost is not classified as a controlled substance by the DEA.
What is the generic name for Preboost?
The generic name for Preboost is benzocaine. There are 12 other brand versions of benzocaine.
What is the NDC code for Preboost 4 g/100mL?
The NDC (National Drug Code) for Preboost 4 g/100mL is 69681-432, listed by The Female Health Company d/b/a Veru Healthcare.
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)